Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.851 0.040 10 62637778 intron variant T/C snv 0.29 0.700 1.000 2 2018 2019
Basal Cell Cancer
CUI: C0751676
Disease: Basal Cell Cancer
109 0.851 0.040 10 62637778 intron variant T/C snv 0.29 0.700 1.000 1 2017 2017
Basal cell carcinoma
CUI: C0007117
Disease: Basal cell carcinoma
109 0.851 0.040 10 62637778 intron variant T/C snv 0.29 0.700 1.000 1 2017 2017
Basal Cell Neoplasm
CUI: C0206710
Disease: Basal Cell Neoplasm
109 0.851 0.040 10 62637778 intron variant T/C snv 0.29 0.700 1.000 1 2017 2017
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.851 0.040 10 62637778 intron variant T/C snv 0.29 0.010 1.000 1 2017 2017
Experimental Organism Basal Cell Carcinoma
63 0.851 0.040 10 62637778 intron variant T/C snv 0.29 0.010 1.000 1 2017 2017